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山竹堿通过破坏多胺积累增强卡泊芬净的抗真菌活性。

Mangiferin enhances the antifungal activities of caspofungin by destroying polyamine accumulation.

机构信息

Shanghai Skin Disease Hospital, Tongji University School of Medicine , Shanghai, P.R. China.

School of Pharmacy, Second Military Medical University , Shanghai, P.R. China.

出版信息

Virulence. 2021 Dec;12(1):217-230. doi: 10.1080/21505594.2020.1870079.

Abstract

The incidence of fungal infections has increased continuously in recent years. Caspofungin (CAS) is one of the first-line drugs for the treatment of systemic fungal infection. However, the emerging CAS-resistant clinical isolates and high economic cost for CAS administration hamper the wide application of this drug. Thus, the combined administration of CAS with other compounds that can enhance the antifungal activity and reduce the dose of CAS has gained more and more attention. In this study, we investigated the effect of mangiferin (MG) on the antifungal activities of CAS. Our results showed that MG acted synergistically with CAS against various ., including CAS-resistant . Moreover, MG could enhance the activity of CAS against biofilm. The synergism of MG and CAS was further confirmed in a mouse model of disseminated candidiasis. To explore the mechanisms, we found that SPE1-mediated polyamine biosynthesis pathway was involved in the fungal cell stress to caspofungin. Treatment of CAS alone could stimulate SPE1 expression and accumulation of polyamines, while combined treatment of MG and CAS inhibited SPE1 expression and destroyed polyamine accumulation, which might contribute to increased oxidative damage and cell death. These results provided a promising strategy for high efficient antifungal therapies and revealed novel mechanisms for CAS resistance.

摘要

近年来,真菌感染的发病率持续上升。卡泊芬净(CAS)是治疗系统性真菌感染的一线药物之一。然而,新兴的 CAS 耐药临床分离株和 CAS 给药的高昂经济成本阻碍了该药物的广泛应用。因此,将 CAS 与其他能增强抗真菌活性并降低 CAS 剂量的化合物联合给药越来越受到关注。在这项研究中,我们研究了芒果苷(MG)对 CAS 抗真菌活性的影响。结果表明,MG 与 CAS 对各种真菌具有协同作用,包括 CAS 耐药真菌。此外,MG 可增强 CAS 对生物膜的活性。MG 和 CAS 的协同作用在播散性念珠菌病的小鼠模型中得到进一步证实。为了探索其机制,我们发现 SPE1 介导的多胺生物合成途径参与了真菌细胞对卡泊芬净的应激反应。单独使用 CAS 处理可刺激 SPE1 表达和多胺积累,而 MG 和 CAS 的联合处理可抑制 SPE1 表达并破坏多胺积累,这可能导致氧化损伤和细胞死亡增加。这些结果为高效抗真菌治疗提供了一种有前景的策略,并揭示了 CAS 耐药的新机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a9/7801120/56de43a9e259/KVIR_A_1870079_F0001_B.jpg

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